Tergus is more than just a CDMO. We work with your team as an extension of your own laboratory and/or commercial operations, allowing you to leverage Tergus’ technical leadership in topical development and benefit from Tergus’ comprehensive expertise from semi-solid concept to commercialization
For drug product design and development, the Tergus team uses strategic planning, Quality by Design (QbD), and risk-based approaches to help you identify “Go/No Go” decisions earlier and avoid unnecessary costs and delays
For commercial manufacturing, Tergus has built on nearly a decade of regulatory, pre-clinical, and clinical manufacturing experience specifically for topical pharmaceuticals.
Tergus has engaged in topical pharmaceutical research, drug development, testing, and manufacturing for nearly a decade.
Tergus excels in advanced testing methodologies and possesses one of the largest banks of IVRT Franz Diffusion cells in the world.
Tergus can help you remove barriers and risk from your drug development and commercial manufacturing efforts.
Tergus meets you where you are and can take you wherever you need to go.
Focus on Topicals
Tergus’ primary focus is topical, semi-solid pharmaceutical product development, formulation, analysis, testing, cGMP clinical supply and commercial manufacturing.
Tergus helps clients develop novel formulations and platform technologies that provide a competitive edge.
Intellectual Property Generation
Tergus helps its clients develop IP that adds value and maximizes market advantage.
Highly efficient and flexible manufacturing operations allows Tergus to handle a wide range of manufacturing volumes.
Globally Recognized Expertise
Tergus was founded by Dr. Vijendra Nalamothu, who is an expert in the field of dermatology drug development and analysis. Dr. Nalamothu has worked for decades with early-stage compounds, evaluating their feasibility for topical drug products.
Regulatory Scope of Services
The Tergus team includes a veteran group of regulatory experts with extensive experience in regulatory compliance across the product lifecycle, from early and late stage development to clinical trials to scale up and commercial manufacturing.